Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome

The Metabolic Basis of Inherited Disease.

1988 • 7,933 citations

The Metabolic Basis of Inherited Disease.

1972 • 1,407 citations

The assay of arylsulphatases A and B in human urine

1959 • 624 citations

Heritable Disorders of Connective Tissue.

1973 • 518 citations

Hurler's syndrome, an a-L-iduronidase deficiency

1972 • 135 citations

Abnormal Sulphatase Activities in Two Human Diseases (Metachromatic Leucodystrophy and Gargoylism)

1964 • 121 citations

Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)

1973 • 118 citations

Mammalian α-Acetylglucosaminidase. Enzymic Properties, Tissue Distribution, and Intracellular Localization^*

1967 • 92 citations

Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfatase

1974 • 89 citations

The Sulfation of Chondroitin Sulfate in Embryonic Chick Cartilage Epiphyses

1969 • 89 citations

Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblasts

1974 • 86 citations

Hunter's syndrome: A deficiency of L-idurono-sulfate sulfatase

1973 • 86 citations

Sanfilippo A Syndrome SULFAMIDASE DEFICIENCY IN CULTURED SKIN FIBROBLASTS AND LIVER

1974 • 62 citations